HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31238Erstellt: 23. Oktober 2026
Hydrochloric Acid → 3-(4-Methoxyphenyl)-2-phenylprop-2-enoic acid
https://huagongshe.com/de/reaction/31238
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Phenylacetic Acid | HCID 999 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetic Anhydride | HCID 7918 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 3-(4-Methoxyphenyl)-2-phenylprop-2-enoic acid | HCID 236698 | — |
Reaktionsschritte
Triethylamine was added to solution of p-anisaldehyde (10 g) and phenylacetic acid (10 g) in acetic anhydride (25 ml). Reaction mixture was stirred at 90° C. for 8 h. Reaction mixture was cooled and water (600 ml) solution of potassium carbonate (81 g) was added. After addition reaction mixture was heated at 60° C. for an hour. Before neutralising with concentrated hydrochloric acid the reaction mixture was cooled below 10° C. Precipitate was filtered and washed with water. 1H-NMR (400 MHz, d6-DMSO): 12.6 (bs, 1H), 7.67 (s, 1H), 7.4-7.3 (m, 3H), 7.2-7.1 (m, 2H), 7.0-6.9 (m, 2H), 6.8-6.7 (m, 2H), 3.70 (s, 3H). (M)+=254 (100%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07425568B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-eb11651813c84c2689f6df85f5f39bf2 |
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| Quellennotiz | uspto-grants-2008_09 |
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